PL102659B1 - Sposob wytwarzania kopolimerow nitrylowych - Google Patents
Sposob wytwarzania kopolimerow nitrylowych Download PDFInfo
- Publication number
- PL102659B1 PL102659B1 PL1975184056A PL18405675A PL102659B1 PL 102659 B1 PL102659 B1 PL 102659B1 PL 1975184056 A PL1975184056 A PL 1975184056A PL 18405675 A PL18405675 A PL 18405675A PL 102659 B1 PL102659 B1 PL 102659B1
- Authority
- PL
- Poland
- Prior art keywords
- nitrile
- weight
- carbon atoms
- olefinically unsaturated
- copolymers
- Prior art date
Links
- 229920001577 copolymer Polymers 0.000 title claims description 18
- 238000004519 manufacturing process Methods 0.000 title description 3
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Chemical compound C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 claims description 26
- 238000000034 method Methods 0.000 claims description 15
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims description 12
- 150000002825 nitriles Chemical class 0.000 claims description 10
- 125000000217 alkyl group Chemical group 0.000 claims description 8
- 230000035699 permeability Effects 0.000 claims description 8
- 239000002253 acid Substances 0.000 claims description 7
- 150000002148 esters Chemical class 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- 239000007789 gas Substances 0.000 claims description 5
- 150000001875 compounds Chemical class 0.000 claims description 3
- 239000000839 emulsion Substances 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
- 239000011347 resin Substances 0.000 claims description 2
- 229920005989 resin Polymers 0.000 claims description 2
- 125000005843 halogen group Chemical group 0.000 claims 2
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims 1
- 229910001882 dioxygen Inorganic materials 0.000 claims 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 1
- 239000003999 initiator Substances 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
- 239000000203 mixture Substances 0.000 description 10
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 8
- 239000004615 ingredient Substances 0.000 description 8
- 239000000178 monomer Substances 0.000 description 7
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 6
- 238000005452 bending Methods 0.000 description 6
- 238000007334 copolymerization reaction Methods 0.000 description 6
- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 description 6
- 239000001301 oxygen Substances 0.000 description 6
- 229910052760 oxygen Inorganic materials 0.000 description 6
- 238000006116 polymerization reaction Methods 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 5
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 5
- 239000002994 raw material Substances 0.000 description 5
- IANQTJSKSUMEQM-UHFFFAOYSA-N 1-benzofuran Chemical compound C1=CC=C2OC=CC2=C1 IANQTJSKSUMEQM-UHFFFAOYSA-N 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- -1 acrylonitrile Chemical class 0.000 description 4
- MPFMFFPEMCAIKK-UHFFFAOYSA-N C=CC#N.COC(=O)C=C.C1=CC=C2CC=CC2=C1 Chemical group C=CC#N.COC(=O)C=C.C1=CC=C2CC=CC2=C1 MPFMFFPEMCAIKK-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000011888 foil Substances 0.000 description 3
- 229940087305 limonene Drugs 0.000 description 3
- 235000001510 limonene Nutrition 0.000 description 3
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 230000015271 coagulation Effects 0.000 description 2
- 238000005345 coagulation Methods 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 150000002431 hydrogen Chemical group 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000012815 thermoplastic material Substances 0.000 description 2
- LRTOHSLOFCWHRF-UHFFFAOYSA-N 1-methyl-1h-indene Chemical compound C1=CC=C2C(C)C=CC2=C1 LRTOHSLOFCWHRF-UHFFFAOYSA-N 0.000 description 1
- UMFYBZHBGXHDPX-UHFFFAOYSA-N 1h-indene;prop-2-enoic acid Chemical compound OC(=O)C=C.C1=CC=C2CC=CC2=C1 UMFYBZHBGXHDPX-UHFFFAOYSA-N 0.000 description 1
- OYUNTGBISCIYPW-UHFFFAOYSA-N 2-chloroprop-2-enenitrile Chemical compound ClC(=C)C#N OYUNTGBISCIYPW-UHFFFAOYSA-N 0.000 description 1
- IONFARCGGIOTGH-UHFFFAOYSA-N 2-methylprop-2-enoic acid;propyl prop-2-enoate Chemical class CC(=C)C(O)=O.CCCOC(=O)C=C IONFARCGGIOTGH-UHFFFAOYSA-N 0.000 description 1
- RWHRFHQRVDUPIK-UHFFFAOYSA-N 50867-57-7 Chemical compound CC(=C)C(O)=O.CC(=C)C(O)=O RWHRFHQRVDUPIK-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 241000283690 Bos taurus Species 0.000 description 1
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical class CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 241001673391 Entandrophragma candollei Species 0.000 description 1
- 241001436793 Meru Species 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 229910052783 alkali metal Chemical group 0.000 description 1
- 150000001340 alkali metals Chemical group 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical class CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 150000001720 carbohydrates Chemical class 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- WNAHIZMDSQCWRP-UHFFFAOYSA-N dodecane-1-thiol Chemical compound CCCCCCCCCCCCS WNAHIZMDSQCWRP-UHFFFAOYSA-N 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 238000007720 emulsion polymerization reaction Methods 0.000 description 1
- CVUNPKSKGHPMSY-UHFFFAOYSA-N ethyl 2-chloroprop-2-enoate Chemical compound CCOC(=O)C(Cl)=C CVUNPKSKGHPMSY-UHFFFAOYSA-N 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- LNCPIMCVTKXXOY-UHFFFAOYSA-N hexyl 2-methylprop-2-enoate Chemical class CCCCCCOC(=O)C(C)=C LNCPIMCVTKXXOY-UHFFFAOYSA-N 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- NASFKTWZWDYFER-UHFFFAOYSA-N sodium;hydrate Chemical group O.[Na] NASFKTWZWDYFER-UHFFFAOYSA-N 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/42—Nitriles
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US525377A US3926871A (en) | 1974-11-20 | 1974-11-20 | Polymerizates of olefinic nitriles |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PL102659B1 true PL102659B1 (pl) | 1979-04-30 |
Family
ID=24092994
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL1975184056A PL102659B1 (pl) | 1974-11-20 | 1975-10-17 | Sposob wytwarzania kopolimerow nitrylowych |
Country Status (31)
| Country | Link |
|---|---|
| US (1) | US3926871A (fr) |
| JP (1) | JPS5165191A (fr) |
| AR (1) | AR210866A1 (fr) |
| AT (1) | AT341774B (fr) |
| BE (1) | BE833896A (fr) |
| BG (1) | BG31076A3 (fr) |
| BR (1) | BR7507246A (fr) |
| CA (1) | CA1053844A (fr) |
| CH (1) | CH618194A5 (fr) |
| CS (1) | CS191282B2 (fr) |
| DD (1) | DD120451A5 (fr) |
| DE (1) | DE2541430A1 (fr) |
| DK (1) | DK414675A (fr) |
| EG (1) | EG12107A (fr) |
| ES (1) | ES441678A1 (fr) |
| FI (1) | FI59113C (fr) |
| FR (1) | FR2292008A1 (fr) |
| GB (1) | GB1490448A (fr) |
| IE (1) | IE42015B1 (fr) |
| IL (1) | IL48118A (fr) |
| IN (1) | IN142519B (fr) |
| IT (1) | IT1042723B (fr) |
| LU (1) | LU73581A1 (fr) |
| NL (1) | NL7511683A (fr) |
| NO (1) | NO144218C (fr) |
| PH (1) | PH12143A (fr) |
| PL (1) | PL102659B1 (fr) |
| RO (1) | RO67251A (fr) |
| SE (1) | SE416304B (fr) |
| TR (1) | TR18867A (fr) |
| ZA (1) | ZA755899B (fr) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3997709A (en) * | 1975-12-24 | 1976-12-14 | Standard Oil Company | Polymerizates of olefinic nitriles |
| US4136246A (en) * | 1976-10-29 | 1979-01-23 | The Standard Oil Company | Thermoplastic acrylonitrile copolymers |
| US4091199A (en) * | 1976-12-20 | 1978-05-23 | The Standard Oil Company | Acrylonitrile-vinyl ether-indene or coumarone polymers |
| US4074038A (en) * | 1976-12-23 | 1978-02-14 | The Standard Oil Company | Acrylonitrile-styrene-indene interpolymers |
| US4077947A (en) * | 1977-01-17 | 1978-03-07 | Standard Oil Company | Terpolymers comprising olefinic nitriles, N-vinylimides and indene or coumarone and process for preparing the compositions |
| US4074037A (en) * | 1977-02-28 | 1978-02-14 | The Standard Oil Company | Thermoplastic terpolymers of acrylonitrile, vinyl esters and indene |
| US4195135A (en) * | 1977-10-28 | 1980-03-25 | Standard Oil Company | Thermoplastic nitrile resin blends |
| US4153648A (en) * | 1977-10-28 | 1979-05-08 | The Standard Oil Company | Thermoplastic nitrile resin blends |
| US4603186A (en) * | 1985-10-21 | 1986-07-29 | The Standard Oil Company | Tetrapolymers containing indene |
| EP0245554A3 (fr) * | 1986-05-05 | 1989-03-22 | The Standard Oil Company | Terpolymères contenant de l'indène |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1235526A (fr) * | 1959-05-29 | 1960-07-08 | Houilleres Bassin Du Nord | Procédé pour l'obtention de copolymères indène-acrylonitrile |
-
1974
- 1974-11-20 US US525377A patent/US3926871A/en not_active Expired - Lifetime
-
1975
- 1975-09-12 SE SE7510223A patent/SE416304B/xx unknown
- 1975-09-15 CA CA235,461A patent/CA1053844A/fr not_active Expired
- 1975-09-16 ZA ZA00755899A patent/ZA755899B/xx unknown
- 1975-09-16 NO NO753150A patent/NO144218C/no unknown
- 1975-09-16 DK DK414675A patent/DK414675A/da unknown
- 1975-09-16 FI FI752583A patent/FI59113C/fi not_active IP Right Cessation
- 1975-09-16 GB GB37994/75A patent/GB1490448A/en not_active Expired
- 1975-09-16 IN IN1776/CAL/1975A patent/IN142519B/en unknown
- 1975-09-17 DE DE19752541430 patent/DE2541430A1/de not_active Withdrawn
- 1975-09-17 IL IL48118A patent/IL48118A/xx unknown
- 1975-09-17 RO RO7583408A patent/RO67251A/fr unknown
- 1975-09-18 IE IE2055/75A patent/IE42015B1/en unknown
- 1975-09-18 PH PH17591A patent/PH12143A/en unknown
- 1975-09-18 FR FR7528662A patent/FR2292008A1/fr active Granted
- 1975-09-19 IT IT27458/75A patent/IT1042723B/it active
- 1975-09-23 AT AT727575A patent/AT341774B/de active
- 1975-09-23 TR TR18867A patent/TR18867A/xx unknown
- 1975-09-24 DD DD188521A patent/DD120451A5/xx unknown
- 1975-09-24 CH CH1242475A patent/CH618194A5/de not_active IP Right Cessation
- 1975-09-26 BE BE160440A patent/BE833896A/fr unknown
- 1975-09-30 BG BG7531126A patent/BG31076A3/xx unknown
- 1975-10-03 NL NL7511683A patent/NL7511683A/xx not_active Application Discontinuation
- 1975-10-10 ES ES441678A patent/ES441678A1/es not_active Expired
- 1975-10-11 AR AR260638A patent/AR210866A1/es active
- 1975-10-14 LU LU73581A patent/LU73581A1/xx unknown
- 1975-10-16 JP JP50125232A patent/JPS5165191A/ja active Pending
- 1975-10-17 PL PL1975184056A patent/PL102659B1/pl unknown
- 1975-10-27 CS CS757236A patent/CS191282B2/cs unknown
- 1975-11-04 BR BR7507246*A patent/BR7507246A/pt unknown
- 1975-11-09 EG EG75657A patent/EG12107A/xx active
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| PL102659B1 (pl) | Sposob wytwarzania kopolimerow nitrylowych | |
| WO2014062426A1 (fr) | Polymérisation radicalaire contrôlée de monomères (méth)acryliques | |
| JPS62256805A (ja) | 熱可塑性に加工可能なポリメタクリレ−ト成形材料、その製法及びこの成形材料から成る押出成形したプレ−ト及びシ−ト、射出成形部品、成形体及び工作材料部品 | |
| FI59606B (fi) | Polymer anvaendbar som termoplastmaterial vilken bildats av olefinnitril- olefinester- inden- eller kumaron- och diengummienheter | |
| SU496738A3 (ru) | Способ получени водорастворимых термореактивных сополимеров | |
| CN101081885A (zh) | 聚二甲基二烯丙基氯化铵的制备方法 | |
| JPH03181507A (ja) | 結合アクリロニトリル分の高い選択された最終組成を有するアクリロニトリルブタジエンゴムコポリマー及びその連続的重合法 | |
| PL102870B1 (pl) | Sposob wytwarzania kopolimerow nitrylowych | |
| JPS6341517A (ja) | 熱可塑性共重合体の製造方法 | |
| CN108359061B (zh) | 一种含酸酐基团的接枝共聚物及其制备方法和应用 | |
| JPS6390515A (ja) | 耐熱性樹脂組成物の製造方法 | |
| JPS58217501A (ja) | 新規共重合体 | |
| CN1052248C (zh) | 可熔融加工的丙烯腈／甲基丙烯腈共聚物制成的薄膜和纤维 | |
| US3060156A (en) | Polymeric sulfonium salts | |
| CA1241497A (fr) | Preparation de polymeres pulverulents, et leur emploi | |
| US4081592A (en) | Process of polymerizing acrylonitrile copolymers employing terpinolene or gamma terpinene as a chain modifier | |
| JPS6323949A (ja) | 樹脂組成物 | |
| JPH0535725B2 (fr) | ||
| EP0042938A1 (fr) | Homopolymères et copolymères des sels de 1,3-dialkyl-2-alcénylimidazolium | |
| KR20170062792A (ko) | 내열성 공중합체의 제조방법 | |
| KR800001071B1 (ko) | 올레핀성 니트릴류와 디엔 고무류의 중합체수지 조성물 | |
| BG63505B1 (bg) | Формовъчна смес, метод за получаване и използването й | |
| KR790001986B1 (ko) | 올레핀성 니트릴의 중합체 조성물 | |
| CN1268660C (zh) | 含顺丁烯二酸酐共聚物的聚合方法 | |
| SU463264A3 (ru) | Способ получени полимерной композиции |